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A Systems Pharmacology Approach to Determine Active Compounds and Action Mechanisms of Xipayi KuiJie'an enema for Treatment of Ulcerative colitis
被引:25
|作者:
Yu, Wei
[1
]
Li, Zhihong
[4
]
Long, Fei
[1
]
Chen, Wen
[1
]
Geng, Yurong
[1
]
Xie, Zhiyong
[2
]
Yao, Meicun
[3
]
Han, Bo
[1
]
Liu, Teigang
[4
]
机构:
[1] Xinjiang Shihezi Univ, Sch Pharm, Xinjiang 832002, Peoples R China
[2] Shihezi Univ, Affiliated Hosp 1, Sch Med, Xinjiang 832002, Peoples R China
[3] Sun Yat Sen Univ, Coll Pharm, Guangzhou 510006, Guangdong, Peoples R China
[4] DongZhiMen Hosp, Key Lab Chinese Internal Med Educ, Beijing 100070, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
NF-KAPPA-B;
RECEPTOR-GAMMA;
PPAR-GAMMA;
EXPRESSION;
ROSIGLITAZONE;
INFLAMMATION;
PROTECTION;
MEDICINE;
D O I:
10.1038/s41598-017-01335-w
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Xipayi Kui Jie'an (KJA), a type of traditional Uygur medicine (TUM), has shown promising therapeutic effects in Ulcerative colitis (UC). Owing to the complexity of TUM, the pharmacological mechanism of KJA remains vague. Therefore, the identification of complex molecular mechanisms is a major challenge and a new method is urgently needed to address this problem. In this study, we established a feasible pharmacological model based on systems pharmacology to identify potential compounds and targets. We also applied compound-target and target-diseases network analysis to evaluate the action mechanisms. According to the predicted results, 12 active compounds were selected and these compounds were also identified by HPLC-ESI-MS/MS analysis. The main components were tannins, this result is consistent with the prediction. The active compounds interacted with 22 targets. Two targets including PTGS2 and PPARG were demonstrated to be the main targets associated with UC. Systematic analysis of the constructed networks revealed that these targets were mainly involved in NF-kappa B signaling pathway. Furthermore, KJA could also regulate the CD4 + CD25 + Foxp3 + Treg cells. In conclusion, this systems pharmacology-based approach not only explained that KJA could alleviate the UC by regulating its candidate targets, but also gave new insights into the potential novel therapeutic strategies for UC.
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页数:16
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